EP0571831B1 - Procédé en plusieurs étapes de préparation d'élastomères de polyuréthane thermoplastiquement façonnables - Google Patents

Procédé en plusieurs étapes de préparation d'élastomères de polyuréthane thermoplastiquement façonnables Download PDF

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Publication number
EP0571831B1
EP0571831B1 EP93107823A EP93107823A EP0571831B1 EP 0571831 B1 EP0571831 B1 EP 0571831B1 EP 93107823 A EP93107823 A EP 93107823A EP 93107823 A EP93107823 A EP 93107823A EP 0571831 B1 EP0571831 B1 EP 0571831B1
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Prior art keywords
diisocyanate
prepolymer
reaction
chain extenders
polyurethane elastomers
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EP93107823A
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German (de)
English (en)
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EP0571831A2 (fr
EP0571831A3 (fr
Inventor
Herbert Dipl.-Ing. Heidingsfeld
Wolfgang Dr. Bräuer
Friedemann Dr. Müller
Willi Dr. Meister
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Bayer AG
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Bayer AG
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0895—Manufacture of polymers by continuous processes

Definitions

  • the invention relates to a process for the continuous production of thermoplastically processable polyurethane elastomers by a multi-stage prepolymer / belt process.
  • TPU Thermoplastic polyurethane elastomers
  • TPUs are made up of linear polyols, mostly polyester or polyether, organic diisocyanates and short-chain diols (chain extenders). They can be produced continuously or batchwise. As the best known manufacturing process, the so-called belt process and the extruder process are also used industrially.
  • a prepolymer is produced from an essentially linear polyhydroxyl compound and excess organic diisocyanate at temperatures ⁇ 100 ° C., cooled and fed to a mixing head via a metering pump. There you mix it with a certain amount of a low molecular weight diol.
  • the reaction mixture obtained is transferred to a conveyor belt with heating up to 130 ° C.
  • the reaction product is comminuted and tempered. The long reaction time required for prepolymer formation of 1 to 2 hours is economically disadvantageous in this process.
  • the structural components polyhydroxyl compound, diisocyanate and low molecular weight glycols are introduced into the extruder. These are premixed individually or metered directly into the extruder as a pre-adduct of polyhydroxyl compound and diisocyanate, and the reaction is carried out in the extruder under certain process conditions.
  • the thermoplastic polyurethane thus produced is extruded, cooled and shredded as a strand. Disadvantageous is that the TPUs produced by this process do not have consistently good properties for all fields of application. TPUs of the same composition are transparent by the extrusion process, while they show an opaque appearance by the belt process. Opaque TPUs can be easily processed into foils, while transparent TPUs are less suitable because of their tendency to block.
  • Preferred polyols are polyesters, polyethers, polycarbonates or a mixture of these.
  • Suitable polyetherols can be prepared by reacting one or more alkylene oxides with 2 to 4 carbon atoms in the alkylene radical with a starter molecule which contains two active hydrogen atoms bonded.
  • alkylene oxides are: ethylene oxide, 1,2-propylene oxide, epichlorohydrin and 1,2- and 2,3-butylene oxide. Ethylene oxide, propylene oxide and mixtures of 1,2-propylene oxide and ethylene oxide are preferably used.
  • the alkylene oxides can be used individually, alternately in succession or as mixtures.
  • starter molecules examples include water, amino alcohols, such as N-alkyldiethanolamines, for example N-methyldiethanolamine and diols such as ethylene glycol, 1,3-propylene glycol, 1,4-butanediol and 1,6-hexanediol. If appropriate, mixtures of starter molecules can also be used.
  • Suitable polyetherols are also the hydroxyl-containing polymerization products of tetrahydrofuran.
  • the essentially linear polyetherols preferably have molecular weights of 500 to 5000. They can be used both individually and in the form of mixtures with one another.
  • Suitable polyesterols can be prepared, for example, from dicarboxylic acids having 2 to 12 carbon atoms, preferably 4 to 6 carbon atoms, and polyhydric alcohols.
  • suitable dicarboxylic acids are: aliphatic dicarboxylic acids such as succinic acid, glutaric acid, adipic acid, suberic acid, azelaic acid and sebacic acid and aromatic dicarboxylic acids such as phthalic acid, isophthalic acid and terephthalic acid.
  • the dicarboxylic acids can be used individually or as mixtures, for example in the form of a succinic, glutaric and adipic acid mixture.
  • polyesterols it may be advantageous to use the corresponding dicarboxylic acid derivatives, such as carboxylic acid diesters having 1 to 4 carbon atoms in the alcohol radical, carboxylic acid anhydrides or carboxylic acid chlorides, instead of the dicarboxylic acids.
  • dicarboxylic acid derivatives such as carboxylic acid diesters having 1 to 4 carbon atoms in the alcohol radical, carboxylic acid anhydrides or carboxylic acid chlorides, instead of the dicarboxylic acids.
  • polyhydric alcohols are glycols having 2 to 10, preferably 2 to 6, carbon atoms, such as ethylene glycol, diethylene glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,10-decanediol, 2,2- 1,3-dimethylpropanediol, 1,3-propanediol and dipropylene glycol.
  • the polyhydric alcohols can be used alone
  • esters of carbonic acid with the diols mentioned in particular those with 4 to 6 carbon atoms, such as 1,4-butanediol and / or 1,6-hexanediol, condensation products of ⁇ -hydroxycarboxylic acids, for example ⁇ -hydroxycaproic acid, and preferably polymerization products of lactones, for example, optionally substituted ⁇ -caprolactones.
  • polyesterols used are ethanediol polyadipates, 1,4-butanediol polyadipates, ethanediol-butanediol-1,4-polyadipates, 1,6-hexanediol-neopentylglycol polyadipates, 1,6-hexanediol-1,4-butanediol polyadipates and polycaprolactones.
  • the polyesterols have molecular weights from 500 to 5000.
  • Suitable organic diisocyanates are, for example, aliphatic, cycloaliphatic, araliphatic, heterocyclic and aromatic diisocyanates, such as those e.g. in Justus Liebigs Annalen der Chemie, 562, pages 75 to 136.
  • aliphatic diisocyanates such as hexamethylene diisocyanate
  • cycloaliphatic diisocyanates such as isophorone diisocyanate, 1,4-cyclohexane diisocyanate, 1-methyl-2,4- and -2,6-cyclohexane diisocyanate and the corresponding isomer mixtures
  • 4,4'-, 2,4'- and 2,2'-dicyclohexylmethane diisocyanate and the corresponding isomer mixtures and preferably aromatic diisocyanates such as 2,4-tolylene diisocyanate, mixtures of 2,4- and 2,6-tolylene diisocyanate, 4,4'-, 2,4'- and 2,2'-diphenylmethane diisocyanate, mixtures of 2,4'- and 4,4'-diphenylmethane diisocyanate, urethane-modified liquid 4,4'- and / or 2,4'--
  • diisocyanates mentioned can be used together with up to 15% (calculated on diisocyanate), but at most so much of a polyisocyanate that a thermoplastically processable product is formed.
  • Examples are triphenylmethane-4,4 ', 4 "-triisocyanate and polyphenyl-polymethylene-polyisocyanates.
  • Suitable chain extenders with a molecular weight of 62 to 500 are preferably aliphatic diols with 2 to 14 carbon atoms, such as, for example, ethanediol, 1,6-hexanediol, diethylene glycol, dipropylene glycol and in particular 1,4-butanediol.
  • diesters of terephthalic acid with glycols having 2 to 4 carbon atoms such as, for example, terephthalic acid bis-ethylene glycol or 1,4-butanediol, hydroxyalkylene ethers of hydroquinone, such as, for example, 1,4-di ( ⁇ -hydroxyethyl) hydroquinone, (cyclo ) aliphatic diamines, such as Isophorone diamine, ethylenediamine, 1,2-, 1,3-propylenediamine, N-methyl-propylenediamine-1,3, N, N'-dimethylethylenediamine and aromatic diamines, such as 2,4- and 2,6- Toluylenediamine, 3,5-diethyl-2,4- and / or -2,6-toluenediamine and primary ortho-, di-, tri- and / or tetraalkyl-substituted 4,4'-diaminodiphenylmethanes.
  • the diol chain extenders can be used together with up to 15% (calculated on chain extenders) but at most as much of a triol with a molecular weight of up to 500 that a thermoplastically processable product is produced.
  • examples are glycerol, trimethylolpropane and their low molecular weight alkylene oxide adducts.
  • the structural components if appropriate in the presence of catalysts, auxiliaries and / or additives, can be reacted in such amounts that the equivalence ratio of NCO groups to the sum of the NCO-reactive groups, in particular the OH groups of the low molecular weight diols / Triplets and macrodiols 0.9: 1 to 1.20: 1, preferably 0.95: 1 to 1.10: 1.
  • Suitable catalysts which in particular accelerate the reaction between the NCO groups of the diisocyanates and the hydroxyl groups of the diol components are the tertiary amines known and customary in the prior art, such as triethylamine, dimethylcyclohexylamine, N-methylmorpholine, N, N'-dimethyl -piperazine, 2- (dimethylaminoethoxy) ethanol, diazabicyclo (2,2,2) octane and the like and in particular organic metal compounds such as titanium acid esters, iron compounds, tin compounds, for example tin diacetate, tin dioctate, tin dilaurate or the tin dialkyl salts of aliphatic carboxylic acids such as dibutyltin diacetate or durutyl tin dilautilate.
  • the catalysts are usually used in amounts of 0.0005 to 0.1 part per 100 parts of polyhydroxy compound.
  • auxiliaries and / or additives can also be incorporated into the structural components.
  • auxiliaries and / or additives can also be incorporated into the structural components. Examples include lubricants, inhibitors, stabilizers against hydrolysis, light, heat and discoloration, flame retardants, dyes, pigments, inorganic and / or organic fillers and reinforcing agents.
  • Reinforcing agents are in particular fibrous reinforcing materials such as e.g. inorganic fibers that are manufactured according to the state of the art and can also be supplied with a size.
  • auxiliaries and additives can be found in the specialist literature, for example the monograph by JH Saunders and KC Frisch "High Polymers", Volume XVI, Polyurethane, Parts 1 and 2, Verlag Interscience Publishers 1962 and 1964 or DE-A 2 901 774.
  • thermoplastics for example polycarbonates, polyesters and acrylonitrile butadiene styrene polymers, in particular ABS.
  • elastomers such as e.g. Rubber, ethylene-vinyl acetate polymers, styrene-butadiene copolymers and other TPU's can be used.
  • plasticizers such as e.g. Phosphates, phthalates, adipates, sebacates.
  • stage A The components of stage A are intimately mixed at temperatures above their melting point. This is preferably carried out in a mixing unit with high shear energy.
  • a mixing head preferably a high-speed spike mixer, or a nozzle can be used.
  • the prepolymer reaction (stage B) should essentially be brought to complete conversion. Preferably, more than 80 mol% of polyol should be reacted in this stage.
  • the reaction temperatures are above 100 ° C, preferably between 100 ° C and 250 ° C.
  • a tubular reactor is used, the length of which is dimensioned such that, in interaction with the reaction temperature, the conversion described above is ensured.
  • the length / diameter ratio is preferably between 2: 1 and 20: 1.
  • the reaction must be controlled, for example via the temperature, in such a way that the conversion mentioned is achieved.
  • stages A and B are carried out in an intensely stirred tubular reactor with a length / diameter ratio of 4: 1 to 15: 1.
  • the combination nozzle / tube reactor optionally with stirring, can also be used.
  • stage C the prepolymer produced in stages A and B is mixed with the low molecular weight diol and optionally triol and / or diamine chain extenders.
  • mixing should take place immediately after the prepolymer reaction has largely ended.
  • a mixing unit working with high shear energy is also preferred for this stage. Examples include a mixing head, a nozzle or a screw extruder.
  • the mixture can also be carried out in the last part of the above-mentioned stirred tube reactor after the prepolymer reaction has taken place.
  • step D the reaction mixture prepared in step C is directly and continuously on a support. preferably a conveyor belt, applied where it is allowed to react until the material solidifies.
  • the conveyor belt is preferably passed through a heating zone with a predetermined temperature> 110 ° C. The speed of the conveyor belt is adjusted depending on the heating temperature so that the chain extension reaction is essentially brought to full conversion.
  • the reaction mixture which has solidified on the conveyor belt can be introduced continuously into an extruder.
  • the known extruders e.g. Single-shaft and twin-screw extruders and bus kneaders are used.
  • the temperatures of the extruder housings are chosen so that the solidified reaction mixture is melted, the chain extension reaction is brought to full conversion and the possible incorporation of the above-mentioned auxiliaries or the other components can be carried out with the greatest possible protection of the product.
  • TPUs can be produced in a targeted and controlled manner with only very small property fluctuations due to the optimal conditions in each process stage in a wide range of properties.
  • the products thus obtained have very good mechanical properties and are suitable for the production of injection molded articles and polyurethane films.
  • a poly-butanediol ether with a molecular weight of approx. 1000 100 parts by weight of a poly-butanediol ether with a molecular weight of approx. 1000 were heated to 180 ° C. and metered into a tube equipped with a spike mixer using a gear pump. Using a second gear pump, 50 parts by weight of molten (50 ° C.) 4,4'-diphenylmethane diisocyanate (MDI) were pumped into the same tube.
  • MDI 4,4'-diphenylmethane diisocyanate
  • the tube has a length / diameter ratio of 8.
  • the speed of the mixer was approximately 1500 rpm.
  • the metering rate was set so that the prepolymer mixture referred to the tubular reactor with a conversion 1) of about 95 mol%. Polyether left.
  • the prepolymer was then continuously and briefly mixed intensively in a directly connected mixing head with 10 parts by weight of butanediol (60 ° C.), which were metered in by means of a gear pump.
  • reaction mixture obtained was applied directly to a conveyor belt which ran continuously for about 1 minute through a zone heated at 130.degree.
  • the moldings produced were easy to remove from the mold.
  • the tubular films obtained from the granules were easy to extrude.
  • Example 2 Analogously to Example 1, the poly-butanediol ether was heated to 200 ° C. and converted into the prepolymer in the tubular reactor. The metering rate was increased so that the prepolymer again left the reactor with about 95% conversion.
  • the moldings produced were easy to remove from the mold.
  • the tubular films obtained from the granules were easy to extrude.
  • Example 2 Analogously to Example 1, 100 parts by weight of a 1,4-poly-butanediol adipate having a molecular weight of approximately 2250 and heated to 140 ° C. were reacted with 114 parts by weight of MDI to form the prepolymer. The sales level achieved in the tubular reactor was 98%.
  • the prepolymer was mixed with a mixture of 35 parts by weight of butanediol, 1.75 parts by weight of hexanediol and 1.27 parts by weight of stearyl alcohol.
  • the melt solidified at the end of the conveyor belt was drawn into a twin-screw extruder with a diameter of 53 mm and housing temperatures from 140 ° C to 200 ° C.
  • 1.5 parts by weight of bis-ethylene-stearylamide and 34 parts by weight of an ABS powder were metered in with metering scales.
  • the hot melt was drawn off as a strand, cooled in a water bath and granulated.
  • the moldings produced were easy to remove from the mold.
  • Example 3 100 parts by weight of a 1,4-polybutanediol adipate having a molecular weight of approximately 2250 were converted to 40% by weight of MDI to form the prepolymer in the tubular reactor up to 97%.
  • the prepolymer was mixed with 10.5 parts by weight of butanediol in the mixing head. After the conveyor belt, the strand was drawn into a single-shaft extruder with a diameter of 60 mm and housing temperatures from 180 ° to 220 ° C. The speed was 60 rpm.
  • the moldings produced were easy to remove from the mold.
  • the tubular films obtained from the granules were easy to extrude.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Polyurethanes Or Polyureas (AREA)

Claims (4)

  1. Procédé pour la fabrication continue d'élastomères de polyuréthannes aptes au travail thermoplastique dans un procédé à plusieurs stades, caractérisé en ce que
    A. on mélange un ou plusieurs polyols essentiellement linéaires, de poids moléculaire 500 à 5000, avec un diisocyanate de formule générale OCN-Z-NCO dans laquelle Z représente un radical organique divalent,
    B. on convertit le mélange obtenu au stade A., dans un réacteur, à des températures de réaction supérieures à 100°C, en le prépolymère, dans une réaction essentiellement complète,
    C. on mélange le prépolymère obtenu au stade B. avec des diols et le cas échéant des triols et/ou des diamines à bas poids moléculaire, de poids moléculaire 62 à 500, servant d'agents d'allongement des chaînes, en réglant au total, tenu compte de tous les composants de réaction des stades A., B. et C., à un rapport NCO/H actif de 0,9:1 à 1,2:1,
    D. on transfère le mélange de réaction préparé au stade C. sur un support où on le laisse réagir jusqu'à solidification,
    E. le cas échéant, on fond le mélange de réaction solidifié obtenu au stade D. dans une extrudeuse dans laquelle on mélange des produits auxiliaires et/ou autres composants.
  2. Procédé pour la fabrication d'élastomères de polyuréthannes aptes au travail thermoplastique selon la revendication 1, caractérisé en ce que
    A. on mélange en continu dans un appareil approprié, à haute énergie de cisaillement un ou plusieurs polyesters, polyéthers, polycarbonates essentiellement linéaires ou un mélange de tels composants, de poids moléculaire 500 à 5 000, avec un ou plusieurs diisocyanates choisis parmi le dicyclohexylméthane-diisocyanate, l'isophoronediisocyanate, l'hexaméthylènediisocyanate, le naphtylènediisocyanate ou un mélange d'isomères du diphénylméthane à une teneur supérieure à 96 % en poids en le 4,4'-diphénylméthanediisocyanate, et plus spécialement le 4,4'-diphénylméthanediisocyanate,
    B. on convertit le mélange obtenu au stade A., en continu, dans un réacteur tubulaire ayant un rapport longueur/diamètre de 2:1 à 20:1, à des températures de réaction de 100 à 250°C, en le prépolymère, dans une réaction essentiellement complète,
    C. on mélange en continu le prépolymère préparé au stade B. avec un ou plusieurs agents d'allongement des chaînes choisis parmi l'éthylèneglycol, le butanediol, l'hexanediol, la 1,4-di-(β-hydroxyéthyl)hydroquinone, et le cas échéant des agents d'allongement des chaînes consistant en triols, dans un appareil approprié à haute énergie de cisaillement, en réglant au total, tenu compte de tous les composants de réaction des stades A., B. et C., à un rapport NCO/H actif de 0,95:1 à 1,1:1,
    D. on envoie en continu le mélange de réaction préparé au stade C. sur une bande transporteuse qui le conduit, jusqu'à solidification de la matière, au travers d'une zone de chauffage présentant une température déterminée supérieure ou égale à 110°C,
    E. le cas échéant, on fond le mélange de réaction solidifié obtenu au stade D. dans une extrudeuse dans laquelle on mélange les produits auxiliaires et/ou d'autres composants.
  3. Procédé de préparation d'élastomères de polyuréthannes aptes au travail thermoplastique selon la revendication 1 ou 2, caractérisé en ce que le mélange et la réaction de formation du prépolymère des stades A. et B. sont réalisés ensemble, dans un réacteur tubulaire agité sous haute énergie de cisaillement à un rapport longueur/diamètre de 4:1 à 15:1, à des températures de réaction de 100 à 250°C et avec un taux de conversion supérieur à 80 mol % par rapport au polyol.
  4. Procédé de préparation d'élastomères de polyuréthannes aptes au travail thermoplastiques selon les revendications 1 à 3, caractérisé en ce que, au stade E., dans l'extrudeuse, on introduit en tant qu'autres composants une résine thermoplastique, en particulier un polycarbonate, un polyester et/ou un polymère ABS, ou une matière renforçante, en particulier une fibre minérale, ou bien d'autres élastomères et des plastifiants.
EP93107823A 1992-05-26 1993-05-13 Procédé en plusieurs étapes de préparation d'élastomères de polyuréthane thermoplastiquement façonnables Expired - Lifetime EP0571831B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4217365 1992-05-26
DE4217365A DE4217365A1 (de) 1992-05-26 1992-05-26 Verfahren zur Herstellung von thermoplastisch verarbeitbaren Polyurethan-Elastomeren durch einen mehrstufigen Prozeß

Publications (3)

Publication Number Publication Date
EP0571831A2 EP0571831A2 (fr) 1993-12-01
EP0571831A3 EP0571831A3 (fr) 1994-04-20
EP0571831B1 true EP0571831B1 (fr) 1996-10-23

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EP (1) EP0571831B1 (fr)
DE (2) DE4217365A1 (fr)

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EP0571831A2 (fr) 1993-12-01
US5545707A (en) 1996-08-13
EP0571831A3 (fr) 1994-04-20
DE4217365A1 (de) 1993-12-02
DE59304248D1 (de) 1996-11-28

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